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New · posted Oct 15

Tolmar · Pharmaceuticals

QC Associate I - Incoming

  • Windsor, CO
  • On-site
  • Full-time
  • Associate & Specialist
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Pay$44Ka year · $21.21–$21.21 an hour
ScheduleMon–Fri8am–4:30pm · 8.5-hour shifts
LocationWindsor, COOn-site
LevelAssociate & Specialist
FunctionQuality ControlQuality
Deadline

Open until filled

The role

Purpose and Scope

The Quality Control Associate I - Incoming is responsible for sampling, inspection, testing, and release of  incoming materials and components. They also are the overall Quality support for receiving activities throughout multiple facilities.

What you need

  • High school diploma or GED required.
  • Associate’s degree or college level courses preferred.
  • Experience in a high volume manufacturing environment or laboratory is preferred.

Knowledge, Skills & Abilities

  • Working knowledge in drug or device cGMP.
  • Knowledge of computer operations, including proficiency with MS Word, Excel, powerpoint, and Access.
  • Ability to learn Tolmar’s electronic systems.
  • Skill in organization and attention to detail.
  • Skill in effective written and oral communication.
  • Work independently and properly prioritize tasks with limited supervision.
  • Ability to work well with employees at all levels and departments.
  • Ability to read, understand and follow procedures.
  • Ability to identify non- conforming materials, processes and procedures.
  • Demonstrate competency in technical writing.
  • Ability to use critical thinking to address potential areas of concern.
  • Proficiency in utilization of electronic data management systems.
  • Acceptable MVR required.
  • Ability to bend, squat, and lift minimum of 30 pounds required.
  • Ability to pass physical and eye exam required.
  • Ability see color.

Skills named in this posting

What you'll do

  1. Inspect incoming materials, components, and finished product against specified requirements.
  2. Perform associated physical or dimensional testing on incoming materials including labels, cartons, syringes, containers etc. to ensure compliance with standards (e.g. ISO, ASTM).Operate inspection equipment (calipers, micrometers and optical comparators to evaluate product measurements.
  3. Document all results per cGMP, ALCOA+ and data integrity policies and procedures.
  4. Enter data and results into LIMS.
  5. Review COAs and COCs and other related documentation for all incoming materials, including APIs and excipients for compliance to the specification prior to release of the materials in Tolway for use in production.
  6. Releases product in Tolway for use in production.
  7. Follow procedures to determine status or disposition, and properly document results on records and in laboratory notebooks.
  8. Perform damage assessments for materials and escalate associated quality defects.
  9. Perform inventory requisitions for requesting departments.
  10. Place materials on hold in Tolway related to deviations and for expired materials.
  11. Determine which materials should be placed in a rejected status and segregate non-conforming materials
  12. Determine which materials require retesting.
  13. Ensure proper handling, storage and traceability of approved materials.
  14. Perform inspection, documentation and release of all controlled supplies ensuring the integrity and sterility.
  15. Perform release of nitrogen to be utilized in the aseptic production of Eligard and EPSS.
  16. Review logbooks, and documentation to support room cleans.
  17. Support Materials Management (Receiving and Issuance Personnel) with inspections and material sampling as needed.
  18. Perform required CBT’s, annual data integrity and safety related trainings and cross train on all associated job functions to ensure adequate process coverage.
  19. Complete compliance training according to requirements and maintain training records in the electronic document system.
  20. Ensure proper status and storage of materials and product.
  21. Sample materials for outside departments, supporting stat requests as needed.
  22. Update and review SOPs and work instructions using the electronic document management system.
  23. Collection and disposal of retain samples in accordance with procedures.
  24. Generate document change requests for specifications.
  25. Initiate deviations, complete immediate actions and request assessments for non-conformances from appropriate groups (ie Packaging Engineering).
  26. Attend T3 academy.
  27. Support and participate in reduction in cycle time and cost savings initiatives.
  28. Perform cleaning and monitoring of rooms and equipment.
  29. Coordinate equipment calibration with the instrumentation team.
  30. Collaborate with supplier quality to resolve material quality issues or discrepancies.
  31. Monitor equipment and facilities for proper operating conditions.
  32. Participate in monthly quality and safety walkthroughs.
  33. Perform cross training in other QCC systems, processes and procedures including laboratory support, sample submission, logbook creation, inventory maintenance and glassware cleaning, stability sample pulls and submission to the laboratory.
  34. Wash and dry glassware and distribute to appropriate locations within the laboratory.
  35. Participate in required annual hazardous waste training. Hazardous waste involvement may include, but is not limited to container and tank management and inspections, generation of hazardous waste as a part of production or sampling processes and transfer of hazardous waste between lab procedure area, satellite accumulation and storage. Respond to spills per the Chemical Spill Procedures.
  36. Perform various other duties as assigned.

Pay

$44,117 a year

Employer provided

$21.21 an hour · yearly at 2,080 hours (40 a week)

How this compares

Tolmar compensation programs are focused on equitable, fair pay practices including market-based base pay and a strong benefits package. The final compensation offered may vary from the posted range based on the selected candidates qualifications and experience.

Where you'll work

Windsor, COOn-siteOpen in Maps (opens in a new tab)

More jobs in Windsor, CO

Schedule and working conditions

Days

Hours

Shift5 days a week8.5-hour shifts42.5 hours on site a week

Monday - Friday, 8:00 am - 4:30 pm

  • Working conditions are in an office, warehouse, laboratory and manufacturing environment.
  • Must be adaptable to shifting priorities and operate with a sense of urgency while maintaining high quality in order to meet important timelines in a high throughput environment.
  • Business demands may present a need to work extended hours.
  • Occasional overtime may be required.
  • Work may consist of travel between multiple facilities.

From the posting

About Tolmar

Core Values

  • The QCC Associate is expected to operate within the framework of Tolmar’s Core Values:
  • Center on People:  We commit to support the well-being of our patients. We are committed to treating our employees and those we serve as valued partners. By placing people at the heart of our actions, we actively engage, invigorate, acquire knowledge, and grow together.​
  • Are Proactive & Agile:  We embody a culture of engagement and action. With a hands-on approach, we fearlessly adapt to change. We anticipate, respond swiftly and efficiently to ignite a spirit that propels us towards extraordinary outcomes.​
  • Act Ethically:  We are committed to consistently conducting our business in an ethical, compliant, and socially aware manner, in line with our purpose of positively impacting lives. We actively cultivate diversity, equity, inclusion & sustainability in our workplace.
  • ​Constantly Improve:  We are committed to a collaborative & proactive effort to improve our products, systems, processes, and services by reducing waste, increasing efficiency & improving quality.​
  • Are Accountable:  We think, act, and communicate with honesty, transparency, and clarity in alignment with our core values. We don't compromise our values for near term gain. We take accountability & ownership of our work, actions, successes, and setbacks. We strive to deliver our best as we shape the future.​
Tolmar company page · 9 open roles
Equal opportunity, accessibility and legal noticesTolmar's statements, word for word

Tolmar is an Equal Opportunity Employer. We do not discriminate on the basis age 40 and over, color, disability, gender identity, genetic information, military or veteran status, national origin, race, religion, sex, sexual orientation or any other applicable status protected by state or local law. It is our intention that all qualified applicants be given equal opportunity and that selection decisions are based on job-related factors.

Job intelligence

The context around this role

Live data · October 15, 2026

Salary intelligence

How the pay compares

This role's midpoint is 26% below the US median for Quality Control roles at this level.

This roleEmployer provided

$44,117 to $44,117 a year

Associate & Specialist roles in Colorado6 roles publishing pay

Middle half $47,375 to $76,000, median $63,750

Associate & Specialist roles in the US100 roles publishing pay

Middle half $49,375 to $76,125, median $60,000
Annual base pay
Annual base payLowMedianHigh
This role$44,117—$44,117
Colorado$47,375$63,750$76,000
All US$49,375$60,000$76,125

This role: Tolmar's own published range, converted to a year at 2,080 hours. Comparisons: the base pay employers published on open Quality Control roles at the same level on Regulatory Jobs, October 15, 2026. Nothing is estimated.

Career trajectory

Where this role sits in Quality Control

The general path across 275 open Quality Control roles on Regulatory Jobs, with the titles they carry most. Not Tolmar's own promotion track.

  1. This role

    Associate & Specialist

    Often: Quality Inspector · Quality Control Inspector

    $60K median149 open

  2. Next step

    Senior & Principal

    Often: Scientist, Quality Control · Senior Scientist, Quality Control

    $95K median70 open

  3. Later

    Manager

    Often: Quality Control Manager · Manager Quality Control

    $127K median31 open

  4. Later

    Director

    Often: Associate Director, Quality Control · Senior Director, Quality Control

    $199K median25 open

Skills DNA

What this role leans on

How many of the posting's 56 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.

GMP and compliance: 9 linesLab testing and methods: 9 linesDocumentation and SOPs: 14 linesInvestigations and CAPA: 3 linesRegulatory submissions: 1 lineQuality systems and risk: 1 lineData and digital systems: 6 linesCollaboration and leadership: 7 linesGMPLab testingDocumentationInvestigationsSubmissionsQuality systemsData systemsTeamwork
  • Documentation and SOPs14
  • GMP and compliance9
  • Lab testing and methods9
  • Collaboration and leadership7
  • Data and digital systems6
  • Investigations and CAPA3
  • Regulatory submissions1
  • Quality systems and risk1

Regulatory intelligence

The rules behind this role

Frameworks and standards this posting's work falls under, matched from its own words, each linked to the official source.

From Regulatory News

Manufacturing and quality coverage for this profession

Company hiring pulse

Tolmar on Regulatory Jobs

9
Open roles
8
Distinct roles
2
Locations

By discipline

  • Quality8 89%
  • Compliance & Safety1 11%

By level

  • Senior & Principal4 44%
  • Associate & Specialist4 44%
  • Manager1 11%
See all 9 Tolmar roles

More roles at Tolmar

All 9 Tolmar roles

Similar Quality Control roles elsewhere

QC Associate I - Incoming at Tolmar

Open until filled. $44K a year, employer provided.

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    QC Associate I - Incoming at Tolmar — Windsor, CO | Regulatory Jobs